Poly Maintenance Supervisor at Clairo

West Union, South Carolina, United States

Clairo Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
ManufacturingIndustries

Requirements

  • Bachelor's degree in a technical/business management discipline and 4 years suggested minimum experience, or 2-year degree in a technical discipline and 8 years suggested minimum experience, or equivalent combination of education and experience
  • 4+ years of maintenance experience in a manufacturing facility
  • Strong PLC and electrical control circuits experience, including troubleshooting and familiarity with programming
  • Strong knowledge of injection molding, assembly, heat melts, robotics, and automation
  • Maintenance experience required on electrical, hydraulic, mechanical, and pneumatic troubleshooting
  • Experience with stamping dies, metal forming processes, and equipment
  • Working knowledge of building operating equipment, including lighting, electrical, compressors, chillers, HVAC, etc
  • Preferred: Manufacturing experience
  • RCRA Haz Waste Responsibility Training Required
  • Ownership and supervision of all tasks below in the PF Department: Staff Hazardous Waste Training PP, Correct Disposition of Waste, PF Hazardous Waste Disposition PP, Selecting Correct Haz Waste Packaging, Correct Labeling/Marking/Closing of HW Packaging, Correct use of HW Satellites, Correct use of the Haz Waste Accumulation Area, Responsible for implementing RCRA Contingency Plan

Responsibilities

  • Coordinates the day-to-day activities of Power Frame maintenance team and assists TPM Planner to ensure machinery and production processes function reliably and safely
  • Assists management in development of preventive programs and ensures safety regulations are followed
  • Fully supports TPM initiatives and improvements for the entire facility to increase production capacity
  • Provides direction for maintenance and operations support in a lead (molten metal) processing environment
  • Leads and directs all predictive, preventative, and corrective maintenance activities to allow for efficient operations
  • Analyzes production equipment to prevent costs associated with unexpected machine downtime and to identify opportunities for improvements
  • Assists senior management with plant improvements and expansions
  • Establishes and maintains effective maintenance procedures, including planning, scheduling, material support, and analysis of cost and performance
  • Regularly reviews maintenance methods, manpower utilization, materials, and equipment for potential improvements and cost savings
  • Familiar with KPI data and drives the production environment through the use of data and fact-based findings
  • Directs preventive and predictive maintenance programs to minimize equipment and facility failures using TPM Methodologies
  • Demonstrates understanding and implementation of TPM principles and acts as a mentor to the teams
  • Presents necessary tracking for OEE, MTBF, MTTR, Throughput, Availability, and capacity to upper management and Engineering Manager as directed on a regular basis
  • Coordinates resources between production/engineering to support plant goals daily, weekly, monthly, annually
  • Utilizes CMMS and other data for increased performance decisions
  • Directs stock base and maintenance purchasing operations working with the tool crib supervision and planner to control inventory and establish proper spare parts base
  • Available 24/7 for response to plant breakdowns
  • Manages team across multiple shifts for corrective/call maintenance
  • Provides technical support and staff coordination of maintenance-related items
  • Coordinates all outside maintenance and construction activities
  • Reviews proposals for new equipment, tools, and facilities and plans for installation
  • Assists in preparation, justification, and review of appropriation requests, layout, and equipment changes
  • Establishes standard procedures for operation of all utility facilities and maintains adequate operating records
  • Assists in compliance to pertinent OSHA and EPA regulations
  • Performs other duties as assigned

Skills

TPM
CMMS
Predictive Maintenance
Preventive Maintenance
Corrective Maintenance
OEE
MTBF
MTTR
Maintenance Planning
Scheduling
Inventory Control
KPI Analysis
Leadership
Molten Metal Processing

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters
1972Year Founded
$29.9MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
5,001-10,000Employees

Benefits

Competitive and equitable total rewards package
Physical, mental and financial health and wellness
Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.
The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.
AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.
The company has nearly 50 years of experience in clinical trial technology solutions.
Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.
The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.
Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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